# K071006: Heartway Attendant-Controlled Power Chair, TC1

- Pathway: 510(k) (Traditional)
- Applicant: Heartway Medical Products Co., Ltd.
- Decided: May 21, 2007 after 42 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K022697 (2003). 3 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070489: Heartway Power Tilt Seating System Power Chair, Model# P16RT, Heartway Medical Products Co., Ltd. (2007)

## Most influential descendants
- K111095: Breeze Electric Transport Chair Model 1025 (2011), 1 descendant of its own
- K100327: Heartway Power Chair, P23 (2010), 1 descendant of its own
- K132856: Heartway Power Wheelchair (2014), 0 descendants of its own
- K130517: EZ Transport Chair (2014), 0 descendants of its own
- K120405: Walk on Wheels HS-3500 Electric Aisle Wheelchair (2012), 0 descendants of its own

## Indications for use
The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.

Source page: https://510kreport.com/device/K071006
Methodology: https://510kreport.com/methodology